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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 606351Generated: October 30, 2026

Hexane → HCID 60077543, compound

https://huagongshe.com/reaction/606351

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
ReactantDiisobutylaluminum hydrideHCID 14487—
ReactantEthyl cis-3-bromoacrylateHCID 643842—
Reactant2,5-DifluoroanisoleHCID 2724989—
ReactantButyllithiumHCID 178418339—
Catalystpalladium(II) acetateHCID 167845—
CatalystZincchlorideHCID 3007855—
SolventTetrahydrofuranHCID 8028—
ProductHCID 60077543HCID 6007754392.4%

Reaction Steps

solution of BuLi (2.5M) in hexane (9.6 ml; 0.024 mol) was added to a stirred solution of 2,5-difluoroanisol (2.88 g, 0.02 mol) in dry THF (30 ml) at −70 C, followed after 2 h by solution of zinc chloride (3.6 g; 0.026 mol) in dry THF (50 ml). The reaction temperature was allowed to raise to room temperature and then stirring was maintained at room temperature for 30 min. Pd(OAc)2 (8 mg; 0.2 mol %) was added, followed by ethyl cis-3-bromoacrylate (3.58 g; 0.02 mol). The reaction mixture was placed in preheated oil bath and heated under reflux for 1 h. The resulting reaction mixture was chilled to −78 C and 60 ml (0.06 mol) of DIBAL (1M solution in hexanes) was added dropwise. The stirring was continued at −78 C for 2 h and 1 h at room temperature. The reaction was quenched with water and all solids were dissolved by addition of HCl. The organic phase was diluted with ether, separated, washed with 5N HCl, brine and evaporated in vacuo. The residue was Kugelrohr distilled (1.5×10−2 mbar, 150 C) to give 3.7 g (92%) of crude (2Z)-3-(3,6-difluoro-2-methoxyphenyl)-2-propen-1-ol, which contains˜6% of other regioisomers. The crude product was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07915295B2
Source datasetuspto-grants-2011_03
ORD IDord-c825cee2c7354a49b05bfe7191dff82f
Source noteuspto-grants-2011_03